ClinVar Miner

List of variants in gene FRMPD4 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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Gene type:
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Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_001368397.1(FRMPD4):c.2903C>T (p.Ser968Leu) rs146907470 0.00006
NM_001368397.1(FRMPD4):c.3067T>C (p.Cys1023Arg) rs143929343 0.00006
NM_001368397.1(FRMPD4):c.2048A>G (p.Glu683Gly) rs760597864 0.00004
NM_001368397.1(FRMPD4):c.3938G>A (p.Arg1313Gln) rs759503727 0.00004
NM_001368397.1(FRMPD4):c.3523G>A (p.Asp1175Asn) rs371295955 0.00003
NM_001368397.1(FRMPD4):c.3964+5A>G rs746521307 0.00003
NM_001368397.1(FRMPD4):c.1070+7G>A rs760086099 0.00002
NM_001368397.1(FRMPD4):c.1423G>A (p.Glu475Lys) rs761416670 0.00001
NM_001368397.1(FRMPD4):c.2154C>T (p.Asn718=) rs797045589 0.00001
NM_001368397.1(FRMPD4):c.1682T>C (p.Ile561Thr) rs2147168676
NM_001368397.1(FRMPD4):c.1924G>A (p.Ala642Thr) rs1555897781
NM_001368397.1(FRMPD4):c.2182G>A (p.Ala728Thr) rs750615873
NM_001368397.1(FRMPD4):c.3115C>A (p.Pro1039Thr) rs369963195
NM_001368397.1(FRMPD4):c.3261C>T (p.Arg1087=) rs776961749
NM_001368397.1(FRMPD4):c.42-9C>A rs765633648

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